List of variants in gene combination LOC107982234, WT1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.375C>T (p.Gly125=)	rs776209354	0.00039
NM_024426.6(WT1):c.-106C>T	rs867975105	0.00021
NM_024426.6(WT1):c.381C>G (p.Pro127=)	rs771681406	0.00009
NM_024426.6(WT1):c.615C>G (p.Pro205=)	rs769467940	0.00005
NM_024426.6(WT1):c.27G>A (p.Pro9=)	rs556835183	0.00001
NM_024426.6(WT1):c.75C>T (p.Ser25=)	rs1417997475	0.00001
NM_024426.6(WT1):c.174C>G (p.Leu58=)	rs886048232
NM_024426.6(WT1):c.24C>T (p.Asp8=)
NM_024426.6(WT1):c.390A>C (p.Pro130=)
NM_024426.6(WT1):c.456C>A (p.Gly152=)	rs2133103187
NM_024426.6(WT1):c.543C>T (p.Arg181=)	rs369870529
NM_024426.6(WT1):c.99A>G (p.Pro33=)	rs2133107306

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